Afif Hentati to Humans
This is a "connection" page, showing publications Afif Hentati has written about Humans.
Connection Strength
0.087
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VZV encephalitis that developed in an immunized patient during fingolimod therapy. Neurology. 2015 Jan 06; 84(1):99-100.
Score: 0.017
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Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 2000 Nov 14; 55(9):1388-90.
Score: 0.006
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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 1998 Dec; 2(1):55-60.
Score: 0.006
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[Study of correlation between radiological aspect of pulmonary hydatid cyst and postoperative course]. Rev Pneumol Clin. 2018 Feb; 74(1):35-40.
Score: 0.005
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Familial amyotrophic lateral sclerosis. J Neural Transm Suppl. 1997; 49:219-33.
Score: 0.005
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Molecular genetic basis of familial ALS. Neurology. 1996 Oct; 47(4 Suppl 2):S27-34; discussion S34-5.
Score: 0.005
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Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency. Ann Neurol. 1996 Mar; 39(3):295-300.
Score: 0.005
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Familial amyotrophic lateral sclerosis. Clin Neurosci. 1995-1996; 3(6):338-47.
Score: 0.004
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Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Hum Mol Genet. 1994 Oct; 3(10):1867-71.
Score: 0.004
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Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Hum Mol Genet. 1994 Aug; 3(8):1263-7.
Score: 0.004
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Nat Genet. 1994 Jul; 7(3):425-8.
Score: 0.004
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Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus. Hum Mol Genet. 1992 Jun; 1(3):218.
Score: 0.004
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Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease. Genomics. 1992 Jan; 12(1):155-7.
Score: 0.003
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Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. Am J Hum Genet. 2008 Feb; 82(2):510-5.
Score: 0.003
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Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class. J Med Genet. 2003 Sep; 40(9):e106.
Score: 0.002
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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet. 2001 Oct; 29(2):160-5.
Score: 0.002
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A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis. Neurology. 1997 Jan; 48(1):258-60.
Score: 0.001
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Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31. Hum Mol Genet. 1996 Sep; 5(9):1377-82.
Score: 0.001
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Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group. Neurology. 1996 Jun; 46(6):1507-14.
Score: 0.001
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Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis. Hum Mol Genet. 1995 Jun; 4(6):1113-6.
Score: 0.001
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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science. 1994 Jun 17; 264(5166):1772-5.
Score: 0.001
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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science. 1993 Aug 20; 261(5124):1047-51.
Score: 0.001
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993 Mar 04; 362(6415):59-62.
Score: 0.001
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A molecular genetic approach to amyotrophic lateral sclerosis. Int J Neurol. 1991-1992; 25-26:60-9.
Score: 0.001